Variant report

Variant	nsv456274
Chromosome Location	chr2:35845117-36077340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:35939874-35940327	HepG2	liver:	n/a	n/a
2	CEBPB	chr2:35913520-35913719	A549	lung:	n/a	n/a
3	CEBPB	chr2:35923382-35923646	HepG2	liver:	n/a	chr2:35923513-35923522 chr2:35923513-35923524 chr2:35923491-35923502 chr2:35923511-35923522 chr2:35923511-35923524
4	CEBPB	chr2:35848050-35848250	HepG2	liver:	n/a	chr2:35848175-35848184 chr2:35848174-35848185 chr2:35848173-35848184
5	CEBPB	chr2:36043985-36044121	A549	lung:	n/a	chr2:36044042-36044055 chr2:36044042-36044055
6	CEBPB	chr2:36003004-36003201	A549	lung:	n/a	chr2:36003126-36003135 chr2:36003124-36003135 chr2:36003125-36003136
7	CEBPB	chr2:36068965-36069115	A549	lung:	n/a	chr2:36069021-36069032
8	CEBPB	chr2:36000760-36001020	HepG2	liver:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
9	CEBPB	chr2:35939938-35940319	A549	lung:	n/a	n/a
10	CEBPB	chr2:35966704-35966918	A549	lung:	n/a	n/a
11	CEBPB	chr2:35858519-35858578	K562	blood:	n/a	chr2:35858550-35858561
12	CEBPB	chr2:35933607-35933953	A549	lung:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
13	CEBPB	chr2:35939909-35940320	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:36044031-36044069	HepG2	liver:	n/a	chr2:36044042-36044055 chr2:36044042-36044055
15	CEBPB	chr2:36002964-36003212	HepG2	liver:	n/a	chr2:36003126-36003135 chr2:36003124-36003135 chr2:36003125-36003136
16	CEBPB	chr2:35939861-35940404	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:36068878-36069132	HepG2	liver:	n/a	chr2:36069021-36069032
18	CEBPB	chr2:35870903-35871116	HepG2	liver:	n/a	chr2:35870981-35870992
19	CEBPB	chr2:35858453-35858678	HepG2	liver:	n/a	chr2:35858500-35858513 chr2:35858550-35858561 chr2:35858501-35858512
20	CEBPB	chr2:35931148-35931461	HepG2	liver:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
21	CEBPB	chr2:35933490-35933969	Hela-S3	cervix:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
22	CEBPB	chr2:35849689-35849697	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:35939882-35940380	A549	lung:	n/a	n/a
24	CEBPB	chr2:35966667-35966899	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:35933609-35933943	H1-hESC	embryonic stem cell:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
26	CEBPB	chr2:35939944-35940305	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:36052197-36052252	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:36068970-36069119	IMR90	lung:	n/a	chr2:36069021-36069032
29	CEBPB	chr2:36000765-36000949	A549	lung:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
30	CEBPB	chr2:35884866-35884899	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:36045437-36045810	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr2:36000495-36000514	HepG2	liver:	n/a	chr2:36000495-36000506
33	CEBPB	chr2:35933609-35933948	IMR90	lung:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
34	CEBPB	chr2:36059690-36059857	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:35933608-35933969	HepG2	liver:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
36	CEBPB	chr2:35939980-35940327	K562	blood:	n/a	n/a
37	CEBPB	chr2:36022021-36022040	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:35933650-35933879	MCF-7	breast:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
39	CEBPB	chr2:36012772-36012798	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:36045533-36045869	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr2:35931181-35931345	H1-hESC	embryonic stem cell:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
42	CEBPB	chr2:35966616-35966957	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr2:35951400-35951550	AG10803	skin:	n/a	n/a
44	CTCF	chr2:36008992-36009157	LNCaP	prostate:	n/a	n/a
45	CTCF	chr2:36009040-36009190	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr2:36009000-36009150	HepG2	liver:	n/a	n/a
47	CTCF	chr2:36029839-36029937	Lung_OC	lung:	n/a	n/a
48	CTCF	chr2:36009059-36009101	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr2:36008940-36009090	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:36009037-36009131	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36049853-36049903	GM06990	blood:	n/a
2	chr2:36049853-36049903	HRPEpiC	eye:	n/a
3	chr2:36018275-36018325	AG09319	gingival:	n/a
4	chr2:36018275-36018325	AoSMC	blood vessel:	n/a
5	chr2:36018275-36018325	MCF10A-Er-Src	breast:	n/a
6	chr2:36018275-36018325	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:36049853-36049903	HRE	kidney:	n/a
8	chr2:36018275-36018325	AG04449	skin:	fetal
9	chr2:36018275-36018325	SAEC	small airway:	n/a
10	chr2:36049853-36049903	SK-N-MC	brain:	n/a
11	chr2:36018275-36018325	NH-A	brain:	n/a
12	chr2:36049853-36049903	NB4	blood:	n/a
13	chr2:36049853-36049903	ovcar-3	ovarian:	n/a
14	chr2:36049853-36049903	HepG2	liver:	n/a
15	chr2:36018275-36018325	HIPEpiC	eye:	n/a
16	chr2:36049853-36049903	AG10803	skin:	n/a
17	chr2:36049853-36049903	NHBE	bronchial:	n/a
18	chr2:36049853-36049903	NH-A	brain:	n/a
19	chr2:36049853-36049903	AG04449	skin:	fetal
20	chr2:36018275-36018325	HMEC	breast:	n/a
21	chr2:36018275-36018325	Jurkat	blood:	n/a
22	chr2:36018275-36018325	ECC-1	luminal epithelium:	n/a
23	chr2:36018275-36018325	BJ	skin:	n/a
24	chr2:36049853-36049903	AoSMC	blood vessel:	n/a
25	chr2:36049853-36049903	HMEC	breast:	n/a
26	chr2:36049853-36049903	HIPEpiC	eye:	n/a
27	chr2:36018275-36018325	T-47D	breast:	n/a
28	chr2:36049853-36049903	HUVEC	blood vessel:	n/a
29	chr2:36049853-36049903	ProgFib	skin:	n/a
30	chr2:36018275-36018325	HEEpiC	esophagus:	n/a
31	chr2:36049853-36049903	T-47D	breast:	n/a
32	chr2:36018275-36018325	SK-N-SH_RA	brain:	n/a
33	chr2:36018275-36018325	HepG2	liver:	n/a
34	chr2:36018275-36018325	PFSK-1	brain:	n/a
35	chr2:36018275-36018325	K562	blood:	n/a
36	chr2:36018275-36018325	HCPEpiC	choroid plexus:	n/a
37	chr2:36018275-36018325	PANC-1	pancreas:	n/a
38	chr2:36018275-36018325	AG10803	skin:	n/a
39	chr2:36018275-36018325	A549	lung:	n/a
40	chr2:36018275-36018325	GM12878	blood:	n/a
41	chr2:36049853-36049903	GM12892	blood:	n/a
42	chr2:36018275-36018325	LNCaP	prostate:	n/a
43	chr2:36018275-36018325	HUVEC	blood vessel:	n/a
44	chr2:36049853-36049903	U87	brain:	n/a
45	chr2:36049853-36049903	SK-N-SH_RA	brain:	n/a
46	chr2:36018275-36018325	H1-hESC	embryonic stem cell:	embryo
47	chr2:36018275-36018325	NHDF-neo	bronchial:	n/a
48	chr2:36018275-36018325	HRCEpiC	kidney:	n/a
49	chr2:36049853-36049903	RPTEC	kidney:	n/a
50	chr2:36049853-36049903	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
2	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
3	chr2:35949877..35953265-chr2:35954228..35956588,3	MCF-7	breast:
4	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
5	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
6	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
7	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
8	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
9	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
10	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
11	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
12	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
13	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-6	chr2:35949825-35950208	NONHSAT070075

Variant related genes	Relation type
MRPL50P1	TF binding region
MRPL50P1	CpG island
ENSG00000234587	chromatin interactions

Extended variants
information (count: 7287 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7287 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7573212	chr2:35845117-35845118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572138693	chr2:35845140-35845141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34270779	chr2:35845144-35845145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370769295	chr2:35845170-35845171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539523754	chr2:35845183-35845184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557877824	chr2:35845212-35845213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576220024	chr2:35845213-35845214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531009014	chr2:35845238-35845239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543663448	chr2:35845266-35845267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145629849	chr2:35845312-35845313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562358775	chr2:35845326-35845327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574275012	chr2:35845388-35845389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541776092	chr2:35845416-35845417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369524100	chr2:35845445-35845446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190276391	chr2:35845468-35845469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527312715	chr2:35845481-35845482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148876096	chr2:35845510-35845511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181082855	chr2:35845540-35845541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532434204	chr2:35845552-35845553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143572354	chr2:35845581-35845582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113627558	chr2:35845631-35845632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116761108	chr2:35845768-35845769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535369553	chr2:35845795-35845796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148320970	chr2:35845801-35845802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565731533	chr2:35845809-35845810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79713634	chr2:35845852-35845853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557789980	chr2:35845905-35845906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1439685	chr2:35846006-35846007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs74768662	chr2:35846036-35846037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186644901	chr2:35846085-35846086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574211769	chr2:35846095-35846096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs398060085	chr2:35846143-35846144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541341907	chr2:35846144-35846145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540897276	chr2:35846191-35846192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141619394	chr2:35846224-35846225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114742997	chr2:35846248-35846249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79905466	chr2:35846259-35846260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190639462	chr2:35846274-35846275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565592638	chr2:35846307-35846308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147066211	chr2:35846322-35846323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117163931	chr2:35846373-35846374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529131161	chr2:35846376-35846377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17017066	chr2:35846389-35846390	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565647192	chr2:35846413-35846414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560376712	chr2:35846442-35846443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180787491	chr2:35846483-35846484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs8179828	chr2:35846522-35846523	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570101688	chr2:35846552-35846553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11483637	chr2:35846558-35846559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397951956	chr2:35846564-35846565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35834200-35851800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:35846200-35846400	Enhancers	Lung	lung
3	chr2:35846400-35846600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:35849200-35849600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:35849200-35849800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr2:35849200-35849800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:35849200-35849800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:35860000-35891000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:35876000-35876800	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr2:35876200-35878600	Enhancers	Fetal Intestine Large	intestine
11	chr2:35876600-35877200	Enhancers	Fetal Intestine Small	intestine
12	chr2:35876800-35877200	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr2:35876800-35877200	Enhancers	Small Intestine	intestine
14	chr2:35877000-35877600	Enhancers	Liver	Liver
15	chr2:35891000-35892000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:35901800-35902000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:35902000-35902200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:35902000-35909000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:35902600-35903200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:35902800-35903600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr2:35907400-35907600	Enhancers	Pancreas	Pancrea
22	chr2:35908400-35909200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:35908400-35909200	Enhancers	Fetal Intestine Large	intestine
24	chr2:35909000-35909200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:35909200-35910800	Weak transcription	Fetal Intestine Large	intestine
26	chr2:35910000-35910200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:35910800-35911000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:35910800-35911000	Enhancers	Fetal Intestine Large	intestine
29	chr2:35917800-35918400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:35922800-35923600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:35937200-35955200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:35943200-35943400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:35947200-35947600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:35955000-35955800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr2:35955000-35955800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:35955200-35955400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:35955200-35955800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr2:35955200-35955800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:35955400-35955800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:35955600-35956000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:35959400-35960000	Enhancers	Fetal Muscle Trunk	muscle
42	chr2:35962600-35963800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:35963600-35963800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:35963800-35971600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr2:35963800-35972000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:35971600-35972000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr2:35972000-35972200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr2:35977000-35977200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:35977200-35980000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:35980000-35984600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links